Canonical Allele Identifier: CA467853061

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131281C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255894C>A , CM000671.2:g.133255894C>A	GRCh38
NC_000009.11:g.136131281C>A , CM000671.1:g.136131281C>A	GRCh37
NC_000009.10:g.135121102C>A	NCBI36
NG_006669.1:g.21774G>T
NG_006669.2:g.24322G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.866G>T
ENST00000647353.1:n.54-4742G>T
ENST00000679909.1:c.28+19268G>T	ENSP00000506089.1:n.28+19268G>T
ENST00000453660.3:n.848G>T
ENST00000538324.2:c.834G>T	ENSP00000483018.1:p.Arg278=
ENST00000611156.4:c.834G>T	ENSP00000483265.1:p.Arg278=
NM_020469.2:c.837G>T	NP_065202.2:p.Arg279=
NM_020469.3:c.837G>T	NP_065202.2:p.Arg279=